TW200835936A - Adhesives inhibiting formation of artifacts in polymer based optical elements - Google Patents
Adhesives inhibiting formation of artifacts in polymer based optical elements Download PDFInfo
- Publication number
- TW200835936A TW200835936A TW096136455A TW96136455A TW200835936A TW 200835936 A TW200835936 A TW 200835936A TW 096136455 A TW096136455 A TW 096136455A TW 96136455 A TW96136455 A TW 96136455A TW 200835936 A TW200835936 A TW 200835936A
- Authority
- TW
- Taiwan
- Prior art keywords
- adhesive
- light
- optical
- beam splitter
- plasticizer
- Prior art date
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 74
- 239000000853 adhesive Substances 0.000 title claims abstract description 65
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 65
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 28
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 21
- 229920000642 polymer Polymers 0.000 title claims description 37
- 239000004014 plasticizer Substances 0.000 claims abstract description 60
- 239000000463 material Substances 0.000 claims abstract description 38
- 239000010410 layer Substances 0.000 claims description 45
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 41
- 238000002425 crystallisation Methods 0.000 claims description 34
- 230000008025 crystallization Effects 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 33
- 230000010287 polarization Effects 0.000 claims description 24
- 239000012790 adhesive layer Substances 0.000 claims description 22
- 230000007547 defect Effects 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- -1 ethylene glycol diols Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 11
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 9
- 239000013078 crystal Substances 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 239000011112 polyethylene naphthalate Substances 0.000 claims description 5
- 230000005855 radiation Effects 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 150000002009 diols Chemical class 0.000 claims description 4
- 238000003384 imaging method Methods 0.000 claims description 4
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 claims description 4
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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 3
- 238000013508 migration Methods 0.000 claims description 3
- 230000005012 migration Effects 0.000 claims description 3
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001634 Copolyester Polymers 0.000 claims description 2
- 230000003750 conditioning effect Effects 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 2
- 239000000052 vinegar Substances 0.000 claims 2
- 235000021419 vinegar Nutrition 0.000 claims 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 1
- 229920000265 Polyparaphenylene Polymers 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 235000011037 adipic acid Nutrition 0.000 claims 1
- 239000001361 adipic acid Substances 0.000 claims 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 claims 1
- 230000001143 conditioned effect Effects 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 1
- 238000012634 optical imaging Methods 0.000 abstract description 6
- 239000010408 film Substances 0.000 description 67
- 239000003822 epoxy resin Substances 0.000 description 10
- 229920000647 polyepoxide Polymers 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
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- 229920006223 adhesive resin Polymers 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000012528 membrane Substances 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 4
- 238000004383 yellowing Methods 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000012923 MOF film Substances 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- 239000004990 Smectic liquid crystal Substances 0.000 description 2
- 230000000712 assembly Effects 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005281 excited state Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 238000011002 quantification Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NPSJHQMIVNJLNN-UHFFFAOYSA-N 2-ethylhexyl 4-nitrobenzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=C([N+]([O-])=O)C=C1 NPSJHQMIVNJLNN-UHFFFAOYSA-N 0.000 description 1
- 239000004808 2-ethylhexylester Substances 0.000 description 1
- MBGYSHXGENGTBP-UHFFFAOYSA-N 6-(2-ethylhexoxy)-6-oxohexanoic acid Chemical compound CCCCC(CC)COC(=O)CCCCC(O)=O MBGYSHXGENGTBP-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 101100289061 Drosophila melanogaster lili gene Proteins 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910052691 Erbium Inorganic materials 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 241000282330 Procyon lotor Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000012668 chain scission Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
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- 230000001934 delay Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B27/00—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
- G02B27/28—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00 for polarising
- G02B27/283—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00 for polarising used for beam splitting or combining
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B27/00—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
- G02B27/10—Beam splitting or combining systems
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/48—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
- B29C65/4805—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by the type of adhesives
- B29C65/483—Reactive adhesives, e.g. chemically curing adhesives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00634—Production of filters
- B29D11/00644—Production of filters polarizing
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/04—Prisms
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
- G02B5/3041—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
- G02B5/305—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0018—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
- B29K2995/0026—Transparent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2011/00—Optical elements, e.g. lenses, prisms
- B29L2011/0066—Optical filters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
- C08K5/053—Polyhydroxylic alcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Ophthalmology & Optometry (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Polarising Elements (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Optical Elements Other Than Lenses (AREA)
Abstract
Description
200835936 九、發明說明: 【發明所屬之技術領域】 本發明係關於在包括一偏振光束分光器之光學成像總成 之一多層膜偏振器中抑制光學缺陷之形成。 【先前技術】 偏振光束分光器(PBS)總成可見於多種光學成像總成 中’諸如正面及背面投影系統、投影顯示器、頭戴式顯示 為、虛擬檢視器、抬頭顯示器、光學計算、光學相關及其 他類似光學檢視及顯示系統。PBs總成可包括至少一個多 層反射光學偏振膜(MOF)。一般而言,M〇f為以多層聚合 物為主之膜’其充當偏振器且含有至少兩種不同材料,其 中至少一種材料在單軸定向後展現雙折射。^1〇1?膜夾在兩 個稜鏡之間且起到反射光之特定偏振同時透射垂直偏振的 作用。黏著劑安置於MOF與該等稜鏡中之至少一者之表面 之間以提供PBS總成之結構完整性以及提供光耦合。 PBS總成用途之一個實例為用於矽上液晶(亦即Lc〇s)背 面投影電視系統中。LCOS背面投影電視系統產生相對高 的量之光能及熱量。該等光能階及熱量對pBS總成之衝擊 尤其隨著時間推移可對PB s總成之平均壽命產生顯著反效 應。更特定言之,隨著時間推移,相對高的量之光能及熱 量可降低MOF之透射率。 【發明内容】 像總 仔在對繼繽改艮之需要,藉此可以並不另外損室光』 成之光學效益的方式來延長光學成像總成(尤其< 125223.doc 200835936 使用偏振元件者)之穩定性及/或使用壽命。 本說明書包括一種偏振光束分光器,其包含以聚合物為 主之偏振膜。黏著層安置於偏振膜上且第一光學元件安置 於黏著層上。黏著層包括至少一種結晶抑制增塑劑組份, 該結晶抑制增塑劑組份之量可有效地抑制在偏振膜中產生 光學缺陷之⑴結晶域、(ii)顆粒或(iii)其組合之形成。 在另一悲樣中,本說明書提供一種包含以聚合物為主之 光子兀件及安置於該光學元件上之黏著劑的光學裝置。黏 著d包“吉晶抑制增塑劑組份,該結晶抑制增塑劑組份之 里可有效地抑制在光學元件中產生光學缺陷之⑴結晶域、 (ii)顆粒或(iii)其組合之形成。 、本況明書之又一態樣提供一種包含雙折射膜之偏振光束 刀光态,胃雙折射膜具有複數個第一材料層及複數個第二 材料層。第—材料層包括選自由聚對苯二甲酸乙二酯及聚 對本一甲1乙_§旨與聚萘:甲酸乙二酯之共聚物組成之群 的聚合物。第二材料層包括共聚酯。偏振光束分光器進一 括至夕個稜鏡,其包含鄰接雙折射膜之第一主要 :土底’及安置於第-主要表面與雙折射膜之間的黏 著劑。黏著劑包含至少_種結晶抑制增塑劑,該結晶抑制 增塑劑之量可有效地抑制偏振膜中之結晶及/或顆粒形 成。 ::明書之另一態樣提供一種使以聚合物為主之光學元 <的方法’該方法包含將黏著劑安置於以聚合物為主 之予7L件上。黏著劑包含結晶抑制增塑劑組份,該結晶 125223.doc 200835936 抑制增塑劑組份之量可有效地抑制在相鄰之以聚合物為主 之光學兀件中產生光學缺陷的⑴結晶域、(ii)顆粒或(iii)其 組合的形成。該方法進一步包括使輻射穿過黏著劑及光學 元件,其中抑制在光學元件中形成結晶域及/或顆粒。 【實施方式】 本說明書之一個態樣係關於與以聚合物為主之偏振膜組 合使用之黏著劑,其用以在將該膜用於(例如)包括一類用 於投影系統中之Cartesian偏振光束分光器("PBS”)的光學成 像系統中時避免在該膜中誘發光學缺陷。本發明之尤其適 用實施例闡明在傾向於降低標準PBS總成之穩定性及/或使 用哥命之相對高的光能及熱量條件下經受連續曝露之PBS 的使用。舉例而言,在使用期延長之後,一些M〇F膜在霜 開始在MOF膜中形成之後可能在相對短之時間段内黃化及 炭化。此快速及顯著失效在用於諸如背面投影電視系統之 極其昂貴之投影系統時得到特別關注。 已確定於PBS總成之偏振膜中所形成之霾可受濕度的影 響且較乾燥環境中之平均壽命通常低於較潮濕環境中之平 均壽命。因此,當在該相對高之光輻照度及相關熱量下、 尤其在乾燥條件下操作時,該等PBS總成之平均壽命顯著 地減少。 雖然下文所說明之實施例係在該投影系統之情況下加以 描述,但本發明之原理及範疇並不受此限定。相反地,本 發明係更廣泛地關於尤其適合於與以聚合物為主之光學元 件組合使用之黏著劑,藉此能夠使諸如霾之光學缺陷降至 125223.doc 200835936 最少或消除。因此’本文中所述之光學成像系統例示本發 明所適用之許多不同種類。 圖1說明偏振光束分光器(PBS)總成1〇之一個實施例。 PBS總成為將入射光線分成第一(透射)偏光組份及第二(反 射)偏光組份之光學組件。PBS總成1〇包括以聚合物為主之 薄膜式多層反射偏振膜12 ;至少一個黏附於多層反射偏振 膜12之互相對置之表面與諸如稜鏡16之光學基板之間的黏 著層14,至少一個黏附於多層反射偏振膜丨2之互相對置之 表面與諸如稜鏡20之光學基板之間的黏著層18。pBs總成 10類似於共同讓渡之美國專利第6,486,997號及同在申請中 且共同讓渡之美國專利公開案第2005/0168697A1號中所描 述者。 雖然PBS總成10說明多層反射偏振膜12夾在稜鏡16與2〇 之間’但是應瞭解多層反射偏振膜12可僅黏附至該等光學 稜鏡中之一者之一個表面上。多層反射偏振膜12可充當偏 振器且可含有至少兩種不同材料,其中至少一種材料在單 軸定向後可展現雙折射。 儘管被描繪為包括兩個稜鏡16及2〇,但是PBs總成1〇可 包括任何合適之光學元件,諸如安置於多層反射偏振膜12 之面或兩面上之光學基板或其類似物。稜鏡16及20可由 任何具有適於實現PBS總成之所要目的之折射率的光透射 材料建構。該等稜鏡應具有小於將會對具有所需f數(f_ number)之光束產生全内反射條件之折射率的折射率。雖 」了使用其他材料,但是棱鏡1 6及2〇通常由各向同性材料 125223.doc 200835936 製成。用作稜鏡之典型材料包括(但不限於)陶瓷、玻璃及 聚合物。出於環保目的,更特定種類之玻璃包括不含有氧 化乱仁可含有其他金屬氧化物(諸如氧化硼)之玻璃。更业 型實例為可自Schott, Corp.(Dureya,PA,USA)購得、不含 錯且具有約!.5 84之折射率之市售玻璃N-SK-5。 更特定言之,PBS總成10可具有稜鏡16及稜鏡2〇。稜鏡 16為首先接收來自光源之入射光之稜鏡。黏著劑具有在 PB S總成經受高強度光歷時長期曝光時間時可抑制削弱以 聚合物為主之光學元件之透射率的光學缺陷形成的添加 劑。具有該等添加劑之黏著劑較佳至少置放於最接近光源 之稜鏡16與多層反射偏振膜12之間。 偏振元件 如圖2及圖3中所說明,多層反射偏振膜12為諸如共同讓 渡之美國專利第6,6〇9,795號中所描述之偏振器。其用於辨 別名義上之s偏振光與p偏振光。特定言之,多層反射’偏振 膜12可具雙折射性,且可具有至少兩種具不同折射率之材 料,其中一種材料在單軸定向後展現雙折射。在一個具體 實施例中,多層反射偏振膜12包含安置於黏著層14、18之 間的複數個堆疊交替之第一及第二光透射層22a n(統稱為 22)及24a_n(統稱為24)。雖然多層反射偏振膜12通常可包含 數百層,但是此簡化之說明例示了偏振器之操作原理。第 一及弟一層(22、24)之每一者具備X、y及z方向上之折射 率。舉例而言,第一層22可具有第一組折射率η22χ、n22y、 nnz,且第二層24可各自具有第二組折射率η24χ、η2”及 125223.doc -10- 200835936 n24z 0 多層反射偏振膜12之另一態樣為第一及第二層22、24之 材料起初為各向同性材料(亦即在X、方向上具有大體 上類似之折射率)且單軸定向之後,該等材料中之至少一 者展現雙折射。存在三種可能之組合:⑴第—材料展現雙 折射而第二材料保持各向同性,(2)第一材料保持各向同性 而第二材料展現雙折射,及(3)第-及第二材料兩者皆展現 雙折射。在-較佳實施例中,單軸定向之後,第—材料具 雙折射性且經歷沿伸展方向上折射率之增加而第二材料保 寺各向同性,且第一與第二材料之間的折射率差在伸展方 向上通常介於規定值〇15與〇·25之間。 將瞭解考慮到欲建構之特定光學系統(諸如pBS總成1〇) 斤而之光學性質,多層反射偏振膜12之組成可顯著地變 化。如所述般,本發明之廣泛範疇並不受限於聚合多層反 射偏振膜12之特定組成或其製造方法。因此,此實施例中 對多層反射偏振膜12之描述係用於光學系統。pBS總成1〇 僅為許多可使用之實例中之一者。 在一較佳實施例中,偏振膜具有分別由第一及第二聚合 物製成之弟一及第二層22、24。舉例而言,第一層22可為 相對高指數層而第二層24可為低指數層。該等相對值係指 〜夕層反射偏振膜12之X軸方向所觀測之指數。可使用許 多相對高及低指數聚合材料。在此實施例中,第一層22中 之相對向指數聚合物可為聚萘二甲酸乙二g旨(PEN)膜。低 指數第二層24可為聚對苯二甲酸乙二酯(PET)膜。其他合 125223.doc -11- 200835936 適聚合材料可用作雙折射/各向同性層。可適當地組合及/ 或創造第一及第二層22、24之指數以展現對於實現所尋求 之光學性質之種類及程度(諸如偏振)而言所必需之所要光 學性質。舉例而言,為改良第一或第二層22、24中之至少 一者之光學性質,以已知方式使該層在指定方向上單軸向 地伸展,藉此(例如)第一層22可具有其經改良之總體折射 率。通常可伸展許多低指數聚合材料。一種典型低指數聚 合物膜可為聚對苯二甲酸乙二酯(PET)膜。參照共同讓渡 之美國專利第6,609,795號來描述可用於製造多層反射偏振 膜12之材料之實例。當PET用作相對高指數層時,用作低 指數層之合適聚合物如下所述。可能需要低指數聚合物在 典型PET拉製溫度下單軸定向之後保持各向同性。因此, 低指數聚合物可具有低於PET之玻璃轉移溫度的玻璃轉移 溫度(亦即小於約80°C)。低折射率聚合物可具有一或多種 以下貝·(1)在PET炼融處理溫度下之熱穩定性,(2)uv 穩定性或UVA防護性,(3)相對高透明度(亦即相對高透射 率及低吸收率),(4)足夠接近PET以達到在共擠壓期間之 穩定流動之流變性質,(5)與PET之良好層間黏著性,(〇低 分散度,及(7)無雙折射情況下之可拉伸性(亦即定向之能 力)。本發明涵蓋其他種類之以聚合物為主之光學元件或 偏振器,諸如延遲膜、吸收偏振器、含PEN或含聚碳酸酯 (PC)偏振器、波長板、彩色濾光片、鏡子、彩色反光鏡 (color mirror)及其他合適類型。顯然,其他聚合材料係可 能的,且只要滿足本文中所論述之標準便可使用其他聚合 125223.doc -12- 200835936 物材料作為第一及第二材料層。 黏著劑 亦參照圖2來說明按照本說明書之教示製造之黏著層14 的一個實施例。黏著層14可為用於黏結諸如PBS總成之光 子元> 件之任何合適的光學或透明黏著劑組合物。如在此方 面所使用’ ”透明"意謂透明黏著劑組合物層必須允許入射 幸虽射之一有效部分穿過。本說明書預想其不僅適用於可見 光且意欲包含抑制對超出可見光譜範圍之波長之透射而言 造成缺陷的結晶或顆粒形成。經降至最少或消除之缺陷主 要為因尺寸大於約1〇〇 nm之結晶域及/或顆粒而造成光散 射之霾。散射通常發生在結晶域及/或顆粒之尺寸為約1/4波 長(例如100奈米)時,且因而引起發白之霾產生於偏振膜 中。如本申請案中所使用,術語”結晶域”意謂形成於聚合 物中、足夠大以形成霾之節結且包括為結晶聚合物鏈及/ 或其片段之匯總之節結/顆粒。 本說明書之黏著劑組合物含有一或多種增塑劑組份,該 增塑劑組份之量可有效地抑制主要在PBS總成中之以聚合 物為主之光學元件中形成光學缺陷。雖然論述以聚合物為 主之PBS光學元件,但是應瞭解本發明係關於在黏著劑中 使用一或多種增塑劑組份,該或該等組份充當用於抑制在 任何黏附至黏著劑之以聚合物為主之光學元件中形成相對 大結晶域及/或顆粒(例如尺寸為〇1 μΜ至〇·3 ^%或1〇〇至 3〇〇奈米)的結晶抑制劑。因而,因曝露於特定輻射某一時 間段而引起之結晶及/或顆粒形成所造成之光學缺陷得到抑 125223.doc -13 - 200835936 制。舉例而言’該特定輻射可包括具有在藍色範圍内或超 出藍色範圍之波長(例如長於420 nm之波長)的光,其光強 度顯著地高於偏振膜將在參考背面投影TV中經歷之光強 度。結果,缺陷之減少延長為達到其所要目的之光學元件 之穩定性及/或使用壽命。 透明黏著劑組合物樹脂組合物可以丙烯酸、乙烯基、 _、環氧樹脂或胺基甲酸酯為主。在此實施例中,其可為 可固化樹脂,諸如透明或光學黏著劑樹脂組合物。透明或 光學黏著劑樹脂組合物具有高強度及低黏度且含有允許其 藉由在相對短時間段内曝露於高溫下或曝露於UV及可見 光下之後固化之添加劑。本發明涵蓋其他合適固化劑。透 明黏著劑組合物亦可為壓敏性黏著劑。透明黏著劑樹脂組 合物可包含一或多種量可隨所得組合物之所要性質及用途 而改變之ί哀氧樹脂。在此方面,典型合適環氧透明樹脂包 括(但不限於)選自由多官能或單官能芳族或脂族環氧樹脂 以及含有多官能或單官能芳族或脂族醇或胺之固化劑組成 之群之環氧樹脂。 用於該等PBS系統中之透明黏著劑樹脂組合物除了上文 所述之一或多種增塑劑組份及添加劑以外亦含有其他添加 J該等其他添加劑可包括(例如)諸如激發態抑止劑、抗 ^ 及收劑及自由基捕獲劑之光穩定劑。透明黏 著劑樹脂組合物亦可包含一或多種適量之固化劑。在此實 施例中’透明黏著劑樹脂組合物係以薄層形式安置於表面 其可以諸如棒塗之任何合適方式或以允許擴散之定計 125223.doc • 14 - 200835936 之形式加以塗覆。通常,所塗覆透明黏著劑樹脂組 口 厚度可介於約1 _至約200 μΜ之範_。更通常 地,厚度可介於約10 μΜ至約6〇 _之範圍内。可視組合 物之所要性貝及用途以及組合物之成份而使用透明黏著劑 树月曰、、且口物之其他厚度範圍。若厚度太薄,則能夠遷移至 偏振臈中以便抑制在其中形成光學缺陷之增塑劑不足。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to suppressing the formation of optical defects in a multilayer film polarizer of an optical imaging assembly including a polarizing beam splitter. [Prior Art] A polarized beam splitter (PBS) assembly can be found in a variety of optical imaging assemblies, such as front and back projection systems, projection displays, head-mounted displays, virtual viewers, heads-up displays, optical computing, optical correlation And other similar optical inspection and display systems. The PBs assembly can include at least one multi-layer reflective optical polarizing film (MOF). In general, M〇f is a film based on a multilayer polymer which acts as a polarizer and contains at least two different materials, at least one of which exhibits birefringence after uniaxial orientation. ^1〇1? The film is sandwiched between two turns and acts to reflect the specific polarization of the light while transmitting the vertical polarization. An adhesive is disposed between the surface of the MOF and at least one of the crucibles to provide structural integrity of the PBS assembly and to provide optical coupling. An example of a PBS assembly use is in a liquid crystal (i.e., Lc〇s) rear projection television system. The LCOS rear projection television system produces a relatively high amount of light and heat. The impact of these light levels and heat on the pBS assembly can have a significant adverse effect on the average lifetime of the PB s assembly, especially over time. More specifically, over time, a relatively high amount of light energy and heat can reduce the transmittance of the MOF. SUMMARY OF THE INVENTION It is necessary to extend the optical imaging assembly in a manner that does not directly damage the optical efficiency of the room light (especially < 125223.doc 200835936 using polarizing elements) ) stability and / or service life. The specification includes a polarizing beam splitter comprising a polymer-based polarizing film. The adhesive layer is disposed on the polarizing film and the first optical element is disposed on the adhesive layer. The adhesive layer includes at least one crystallization inhibiting plasticizer component, the amount of the crystallization inhibiting plasticizer component being effective to suppress (1) crystal domains, (ii) particles or (iii) combinations thereof which produce optical defects in the polarizing film. form. In another sad form, the present specification provides an optical device comprising a polymer-based photonic element and an adhesive disposed on the optical element. Adhesive d package "Ji Jing inhibits the plasticizer component, the crystallization inhibiting plasticizer component can effectively suppress (1) crystal domain, (ii) granule or (iii) combination thereof which causes optical defects in the optical element. Further, in another aspect of the present invention, a polarization beam knife optical state comprising a birefringent film having a plurality of first material layers and a plurality of second material layers is provided. The first material layer comprises a selected from the group consisting of Ethylene terephthalate and a polymer of a group consisting of a copolymer of poly(p-methyl) and polyethylene naphthalate. The second material layer comprises a copolyester. The polarizing beam splitter is further included. Up to now, it comprises a first major adjacent to the birefringent film: a soil bottom and an adhesive disposed between the first major surface and the birefringent film. The adhesive comprises at least one crystal inhibiting plasticizer, The amount of crystallization inhibiting plasticizer can effectively inhibit crystallization and/or particle formation in the polarizing film. :: Another aspect of the book provides a method for making a polymer-based optical element < Place the adhesive on the polymer On the 7L piece, the adhesive contains a crystallization inhibiting plasticizer component, and the crystal 125223.doc 200835936 inhibits the amount of the plasticizer component to effectively inhibit optical defects in adjacent polymer-based optical components. Formation of (1) crystalline domains, (ii) particles, or (iii) combinations thereof. The method further includes passing radiation through the adhesive and the optical element, wherein inhibition of the formation of crystalline domains and/or particles in the optical element is inhibited. One aspect of the present specification relates to an adhesive for use in combination with a polymer-based polarizing film for use in, for example, a Cartesian polarizing beam splitter for use in a projection system (" In the optical imaging system of PBS"), optical defects are induced in the film. Particularly suitable embodiments of the present invention illustrate the use of PBS that is subjected to continuous exposure under conditions that tend to reduce the stability of the standard PBS assembly and/or use relatively high light and heat conditions. For example, after prolonged use, some M〇F films may be yellowed and charred in a relatively short period of time after the frost begins to form in the MOF film. This rapid and significant failure has received particular attention when used in extremely expensive projection systems such as rear projection television systems. It has been determined that the enthalpy formed in the polarizing film of the PBS assembly can be affected by humidity and the average life in a drier environment is generally lower than the average life in a relatively humid environment. Thus, the average lifespan of the PBS assemblies is significantly reduced when operating at relatively high levels of light irradiance and associated heat, particularly under dry conditions. Although the embodiments described below are described in the context of the projection system, the principles and scope of the present invention are not limited thereto. In contrast, the present invention is more broadly directed to adhesives that are particularly suitable for use in combination with polymer-based optical components, thereby minimizing or eliminating optical defects such as germanium to 125223.doc 200835936. Thus the optical imaging system described herein exemplifies many different types of applications to which the present invention applies. Figure 1 illustrates an embodiment of a polarizing beam splitter (PBS) assembly. PBS is always an optical component that splits incident light into a first (transmissive) polarizing component and a second (reflective) polarizing component. The PBS assembly 1 〇 includes a polymer-based film-type multilayer reflective polarizing film 12; at least one adhesive layer 14 adhered between mutually opposing surfaces of the multilayer reflective polarizing film 12 and an optical substrate such as 稜鏡16, At least one adhesive layer 18 adhered between mutually opposing surfaces of the multilayer reflective polarizing film 丨2 and an optical substrate such as 稜鏡20. The pBs assembly 10 is similar to that described in U.S. Patent No. 6,486,997, the entire disclosure of which is incorporated herein by reference. Although the PBS assembly 10 illustrates that the multilayer reflective polarizing film 12 is sandwiched between 稜鏡16 and 2〇', it should be understood that the multilayer reflective polarizing film 12 may adhere only to one of the surfaces of the optical iridium. The multilayer reflective polarizing film 12 can act as a polarizer and can contain at least two different materials, at least one of which exhibits birefringence after uniaxial orientation. Although depicted as including two turns 16 and 2, the PBs assembly 1 can include any suitable optical component, such as an optical substrate or the like disposed on the face or both sides of the multilayer reflective polarizing film 12. The crucibles 16 and 20 can be constructed of any light transmissive material having a refractive index suitable for achieving the desired purpose of the PBS assembly. The enthalpy should have a refractive index that is less than the refractive index that will produce total internal reflection conditions for a beam having the desired f-number. Although other materials are used, the prisms 16 and 2 are usually made of isotropic material 125223.doc 200835936. Typical materials used as crucibles include, but are not limited to, ceramics, glass, and polymers. For environmental protection purposes, a more specific type of glass includes glass that does not contain oxidized kernels and may contain other metal oxides such as boron oxide. A more commercial example is available from Schott, Corp. (Dureya, PA, USA), is error free and has about! .5 84 refractive index of commercially available glass N-SK-5. More specifically, the PBS assembly 10 can have 稜鏡16 and 稜鏡2〇.稜鏡 16 is the first to receive the incident light from the light source. The adhesive has an additive which inhibits the formation of optical defects which weaken the transmittance of the polymer-based optical element when the PB S assembly is subjected to high intensity light for a long period of exposure time. The adhesive having the additives is preferably placed at least between the crucible 16 closest to the light source and the multilayer reflective polarizing film 12. Polarizing Element As illustrated in Figures 2 and 3, the multilayer reflective polarizing film 12 is a polarizer such as that described in U.S. Patent No. 6,6,9,795, the disclosure of which is incorporated herein. It is used to distinguish between nominally s-polarized light and p-polarized light. In particular, the multilayer reflective 'polarizing film 12 can be birefringent and can have at least two materials having different refractive indices, one of which exhibits birefringence after uniaxial orientation. In one embodiment, the multilayer reflective polarizing film 12 includes a plurality of stacked first and second light transmissive layers 22a n (collectively 22) and 24a_n (collectively 24) disposed between the adhesive layers 14, 18. . While the multilayer reflective polarizing film 12 can typically comprise hundreds of layers, this simplified illustration illustrates the principle of operation of the polarizer. Each of the first and second layers (22, 24) has a refractive index in the X, y, and z directions. For example, the first layer 22 may have a first set of refractive indices η22χ, n22y, nnz, and the second layer 24 may each have a second set of refractive indices η24χ, η2” and 125223.doc -10- 200835936 n24z 0 multilayer reflection Another aspect of the polarizing film 12 is that the materials of the first and second layers 22, 24 are initially isotropic (i.e., have substantially similar refractive indices in X, direction) and are uniaxially oriented, such At least one of the materials exhibits birefringence. There are three possible combinations: (1) the first material exhibits birefringence while the second material remains isotropic, (2) the first material remains isotropic and the second material exhibits birefringence, And (3) both the first and second materials exhibit birefringence. In the preferred embodiment, after uniaxial orientation, the first material has birefringence and undergoes an increase in refractive index along the extension direction and a second The material is isotropic, and the refractive index difference between the first and second materials is usually between the specified values 〇15 and 〇·25 in the direction of extension. It will be understood that a specific optical system to be constructed is considered (such as pBS assembly 1〇) Optical properties, multi-layer The composition of the reflective polarizing film 12 can vary significantly. As described, the broad scope of the present invention is not limited to the specific composition of the polymeric multilayer reflective polarizing film 12 or its method of manufacture. Thus, the multilayer reflective polarization in this embodiment The description of film 12 is for an optical system. The pBS assembly 1 is only one of many useful examples. In a preferred embodiment, the polarizing film has a first and second polymer, respectively. And the second layer 22, 24. For example, the first layer 22 can be a relatively high index layer and the second layer 24 can be a low index layer. The relative values are the X of the reflective layer 12 of the reflective layer. Indexes observed in the axial direction. A number of relatively high and low index polymeric materials can be used. In this embodiment, the relatively indexable polymer in the first layer 22 can be a polyethylene naphthalate (PEN) film. The low index second layer 24 may be a polyethylene terephthalate (PET) film. Others 125223.doc -11- 200835936 Suitable polymeric materials may be used as the birefringent/isotropic layer. Or create an index of the first and second layers 22, 24 to show what is being achieved The desired optical properties necessary to determine the type and extent of optical properties, such as polarization. For example, to improve the optical properties of at least one of the first or second layers 22, 24, in a known manner The layer extends uniaxially in a specified direction whereby, for example, the first layer 22 can have an improved overall refractive index. A plurality of low index polymeric materials can generally be stretched. A typical low index polymeric film can be agglomerated. Ethylene terephthalate (PET) film. An example of a material that can be used to fabricate the multilayer reflective polarizing film 12 is described with reference to commonly assigned U.S. Patent No. 6,609,795. When PET is used as a relatively high index layer, it is used as a low Suitable polymers for the index layer are as follows. It may be desirable for the low index polymer to remain isotropic after uniaxial orientation at typical PET draw temperatures. Thus, the low index polymer can have a glass transition temperature (i.e., less than about 80 ° C) below the glass transition temperature of PET. The low refractive index polymer may have one or more of the following: (1) thermal stability at PET refining treatment temperature, (2) uv stability or UVA protection, and (3) relatively high transparency (ie, relatively high) Transmittance and low absorptivity), (4) close enough to PET to achieve rheological properties of stable flow during co-extrusion, (5) good interlayer adhesion to PET, (low dispersion, and (7) Stretchability in the absence of birefringence (i.e., ability to orient). The invention encompasses other types of polymer-based optical elements or polarizers, such as retardation films, absorbing polarizers, PEN-containing or polycarbonate-containing (PC) polarizers, wavelength plates, color filters, mirrors, color mirrors, and other suitable types. Obviously, other polymeric materials are possible, and other than the criteria discussed herein can be used. Polymerization 125223.doc -12- 200835936 Materials as the first and second material layers. Adhesives An embodiment of the adhesive layer 14 made in accordance with the teachings of the present specification is also described with reference to Figure 2. The adhesive layer 14 can be used for bonding Such as PBS assembly Any suitable optical or transparent adhesive composition of the photon element>. As used herein, "transparent" means that the layer of transparent adhesive composition must allow for the incidence to pass through one of the effective portions. The present specification contemplates that it is not only suitable for visible light but is intended to include crystallization or particle formation that inhibits defects that cause transmission to wavelengths outside the visible spectral range. The defects that are minimized or eliminated are primarily due to sizes greater than about 1 〇〇 nm. The crystallization domain and/or the particles cause light scattering. The scattering usually occurs when the crystal domain and/or the size of the particles is about 1/4 wavelength (for example, 100 nm), and thus causes blushing to occur in the polarizing film. As used in this application, the term "crystalline domain" means a nodule/particle formed in a polymer that is large enough to form a nodule of the crucible and includes a summary of the crystalline polymer chain and/or its fragments. The adhesive composition of the present specification contains one or more plasticizer components, and the amount of the plasticizer component is effective to suppress the formation of a polymer-based optical component mainly in the PBS assembly. Optical defects. Although polymer-based PBS optical elements are discussed, it is to be understood that the present invention relates to the use of one or more plasticizer components in an adhesive that acts to inhibit any adhesion. Crystalline inhibitors that form relatively large crystalline domains and/or particles (eg, 〇1 μΜ to 〇·3 ^% or 1 〇〇 to 3 〇〇 nanometers) in a polymer-based optical component to the adhesive Thus, optical defects caused by crystallization and/or particle formation caused by exposure to a certain period of radiation are suppressed by 125223.doc -13 - 200835936. For example, 'this specific radiation may include having a blue color. Light in the range or beyond the wavelength of the blue range (eg, longer than 420 nm) has a light intensity that is significantly higher than the light intensity that the polarizing film would experience in the reference backside projection TV. As a result, the reduction in defects is extended to achieve the stability and/or useful life of the optical component for which it is intended. The transparent adhesive composition resin composition may be mainly acrylic acid, vinyl, epoxide, epoxy resin or urethane. In this embodiment, it may be a curable resin such as a transparent or optical adhesive resin composition. The transparent or optical adhesive resin composition has high strength and low viscosity and contains an additive which allows it to be cured by exposure to high temperatures or exposure to UV and visible light for a relatively short period of time. Other suitable curing agents are contemplated by the present invention. The transparent adhesive composition can also be a pressure sensitive adhesive. The transparent adhesive resin composition may comprise one or more amounts of an oxygen resin which may vary depending on the desired properties and use of the resulting composition. In this aspect, typical suitable epoxy transparent resins include, but are not limited to, those selected from the group consisting of polyfunctional or monofunctional aromatic or aliphatic epoxy resins and curing agents containing polyfunctional or monofunctional aromatic or aliphatic alcohols or amines. The group of epoxy resins. The transparent adhesive resin composition for use in such PBS systems may contain other additives in addition to one or more of the plasticizer components and additives described above. These other additives may include, for example, an excited state inhibitor. , light stabilizer for anti-and agent and free radical trapping agent. The transparent adhesive resin composition may also contain one or more appropriate amounts of curing agents. In this embodiment, the 'transparent adhesive resin composition' is disposed in a thin layer on the surface. It may be applied in any suitable manner such as bar coating or in a form that allows diffusion to be determined 125223.doc • 14 - 200835936. Typically, the thickness of the transparent adhesive resin package applied can range from about 1 _ to about 200 μΜ. More typically, the thickness can range from about 10 μΜ to about 6 〇 _. The transparent adhesive is used for the desired composition and the composition of the composition, and the thickness of the composition is used. If the thickness is too thin, it can migrate into the polarization enthalpy to suppress the shortage of plasticizer in which optical defects are formed.
雖"、、:本文中之例示性實施例可在用於傳遞增塑劑之黏著 J之h况下加以描述,但是本發明之原理及範疇並不受限 於此。相反地,本發明係更廣泛地關於可尤其適合用於允 許有效量之增塑劑遷移以藉由阻止或抑制結晶來延遲霾形 成之組合物。該組合物亦可根據本申請案中所用之彼術語 而清楚瞭解。亦應瞭解可諸如藉由塗佈或其他合適方法直 接塗覆增塑劑。 増塑劑 根據本說明書之一個態樣,一或多種增塑劑組份可包括 於黏著劑中。本發明之研究者推斷光學缺陷(諸如霾)係在 多層反射偏振膜12曝露於相對高程度之入射輻射能及熱量 下時誘發於多層反射偏振膜12中。在(例如)lc〇S投影系統 中經歷該等相對咼程度。咸信以聚合物為主之光學元件之 所述缺點係歸因於已引起多層反射偏振膜12經歷由(例如) 已知Nonish裂解及其他反應引起之斷鏈的光通量。結果, 已觀測到此傾向於降低分子量(MW),藉此產生比初始聚 合物鏈更易移動之鏈之裂解區段。推斷該等較低MW區段 隨著時間之推移傾向於濃縮或聚結在多層反射偏振膜12 125223.doc -15- 200835936 中。該濃縮或聚結傾向於在多層反射膜12中產生霾,藉此 削弱多層反射膜12之穩定性及透射率。 輕貍形成亦使光能夠散射,從而允許高強度光更有效地 與聚合物相互作用,此有效地增加損害。較低Mw物質之 提高之移動率及漸增之濃度允許(例如)PET及/或pEN部分 甚至進一步濃縮至該等部分結晶或形成顆粒之程度。進一 步推斷熱量使得較低MW物質之移動增加且使斷裂反應能 夠實現,藉此提高結晶速率。所得顆粒最終生長至在多層 反射偏振膜12中產生當觀測時,發白,之霾之尺寸。 此情形極不同於此類型之聚合物諸如受紫外線輻射時所 、、二歷之典型降解。通常,將黃化視為光/熱誘致降解之第 一光學徵兆且存在基於吸收不期望之光且使薄膜中所得黃 色減至最少之特定對策。舉例而言,1;乂抑制劑可抑制光 學聚合物膜之光降解。然而,本說明書闡明不同對策,其 將阻止因結晶或顆粒形成而產生於PBS總成中之非典型之 霾(亦即發白之霾)。 本發明之結晶抑制劑為增塑劑,其傾向於抑制該等晶體 或顆粒在多層反射偏振膜12中生長。根據本發明,增塑劑 係選自通用群。典型增塑劑之一些實例係由諸如乙二醇、 聚丙二醇、二(乙二醇)乙醚及三乙二醇之二醇、諸如己二 酸二(2-乙基己酯)及苯曱酸二(乙二醇酯)之芳族或脂族酯 及水組成。 該等增塑劑傾向於在黏著層與黏著至其上之多層反射偏 振膜12之間遷移,且由此進入該膜,藉此在相鄰之膜層中 125223.doc -16- 200835936 顯著地減少(例如)ΡΕΤ及/或PEN部分之結晶。增塑劑之量 及遷移能力為延遲霾形成之重要參數。 應瞭解根據本說明書可使用一種以上增塑劑。在一個實 %例中,乙二醇及水皆可使用。吾人認為水藉由將其本身 以物理方式插人於兩種潛在可結晶材料之間,⑻而藉由締 口及位阻作用予以阻礙而防止結晶。可使用増塑劑組份之 其他組合。該等組合之實例包括(但不限於广通用二醇與Although the exemplary embodiments herein can be described in the context of the adhesive for transferring plasticizers, the principles and scope of the present invention are not limited thereto. In contrast, the present invention is more broadly directed to compositions which may be particularly suitable for allowing an effective amount of plasticizer migration to retard erbium formation by preventing or inhibiting crystallization. The composition can also be clearly understood from the terms used in this application. It will also be appreciated that the plasticizer can be applied directly, such as by coating or other suitable means. Plasticizers According to one aspect of the present specification, one or more plasticizer components can be included in the adhesive. The inventors of the present invention have concluded that optical defects, such as germanium, are induced in the multilayer reflective polarizing film 12 when the multilayer reflective polarizing film 12 is exposed to a relatively high degree of incident radiant energy and heat. These relative degrees of embarrassment are experienced in, for example, lc〇S projection systems. The disadvantages of the polymer-based optical components are attributed to the luminous flux that has caused the multilayer reflective polarizing film 12 to undergo chain scission caused by, for example, known Nonish cracking and other reactions. As a result, it has been observed that this tends to lower the molecular weight (MW), thereby producing a cleavage section of the chain which is more mobile than the initial polymer chain. It is inferred that these lower MW segments tend to concentrate or coalesce over time in the multilayer reflective polarizing film 12 125223.doc -15-200835936. This concentration or coalescence tends to generate flaws in the multilayer reflective film 12, thereby weakening the stability and transmittance of the multilayer reflective film 12. Light raccoon formation also allows light to scatter, allowing high intensity light to interact more efficiently with the polymer, which effectively increases damage. The increased mobility and increasing concentration of the lower Mw species allows, for example, the PET and/or pEN fraction to be even further concentrated to the extent that the portions are crystalline or form particles. Further inferring the heat increases the movement of the lower MW species and enables the fracture reaction to be achieved, thereby increasing the rate of crystallization. The resulting particles are finally grown to a size which is generated in the multilayer reflective polarizing film 12 when observed, and then whitish. This situation is very different from the typical degradation of this type of polymer, such as when exposed to ultraviolet radiation. Typically, yellowing is considered the first optical sign of photo/thermal induced degradation and there are specific countermeasures based on absorbing unwanted light and minimizing the yellow color produced in the film. For example, a ruthenium inhibitor inhibits photodegradation of an optical polymer film. However, this specification clarifies different countermeasures that will prevent atypical enthalpy (i.e., blushing) that is produced in the PBS assembly due to crystallization or particle formation. The crystallization inhibitor of the present invention is a plasticizer which tends to inhibit the growth of such crystals or particles in the multilayer reflective polarizing film 12. According to the invention, the plasticizer is selected from the general group. Some examples of typical plasticizers are diols such as ethylene glycol, polypropylene glycol, di(ethylene glycol) diethyl ether and triethylene glycol, such as di(2-ethylhexyl adipate) and benzoic acid. An aromatic or aliphatic ester of bis(ethylene glycol ester) and water. The plasticizer tends to migrate between the adhesive layer and the multilayer reflective polarizing film 12 adhered thereto and thereby enter the film, thereby significantly in the adjacent film layer 125223.doc -16-200835936 Reduce, for example, crystallization of the ruthenium and/or PEN moiety. The amount of plasticizer and migration ability are important parameters for delayed enthalpy formation. It will be appreciated that more than one plasticizer can be used in accordance with the present specification. In a real case, both ethylene glycol and water can be used. We believe that water prevents crystallization by physically inserting itself between two potentially crystallizable materials, (8) by blocking and sterically hindering. Other combinations of plasticizer components can be used. Examples of such combinations include, but are not limited to, broad diols and
水;二醇與與水;及與構成M〇F之聚合物相互作用 之芳族或脂族部分。 七在個所况明實施例中,用於本中請案之透明黏著劑樹 ::且合,包含-或多種以組合物之總重量計至多約99.5重 里的環氧樹脂。本說明書之環氧樹脂組合物可包含 :或多種以組合物之總重量計約75重量%至約%重量。狀 氧樹脂。另夕卜本發明之環氧樹脂組合物可包含一 -夕種以組合物之總重量計約94重量 的環氧樹脂。 里里/。之里 增塑劑可以將獲得所要程产 透日m 一所錄度之防止缺陷形成之量存在於 透月黏者劑樹脂組合物中。 七^ 用於黏者劑材料中之一種结晶 抑制增塑劑組份之量可廣 f、、、 量%鱼^舌b 了廣,乏地改變,但其通常介於約五重 里與3 0重置〇/0之間壶其入 間。 〆甚至"於、力1重量0/〇與約5重量%之 或劑樹脂組合物可含有至多約3.5重㈣ 劑、黏著…, 劑,諸如填料、穩定 J黏者促進劑(例如矽石' 矽烷)、抗氧化劑、自由基捕 125223.doc 17- 200835936 獲劑、激發態抑止劑及uv吸收劑及其類似物,以便降低 環氧樹脂組合物之重量及/或成本、調節黏度、提供額外 之強化、改良環氧樹脂組合物及光學總成之透明度及/或 使PB S總成穩定以免降解。 圖4說明光學成像器系統之一個實施例,其中系統4丨〇包 括光源412,例如具有前向地引導光418之反射器416之弧 光燈414。光源412亦可為固態光源,諸如發光二極體或雷 射光源。系統410亦包括PBS 420,例如本文中所述之單膜 或多膜PBS。具有X偏振(亦即沿平行於X軸之方向偏振)之 光係由帶圓圈之X表示。具有y偏振(亦即沿平行於y軸之方 向偏振)之光係由實心箭頭表示。實線表示入射光,而虛 線表示已被反射成像器426反射回來、具有經改變之偏振 態之光。可在照明PBS 420之前用調節光學器件422來調節 光源412所提供之光。調節光學器件422將光源412所發出 之光之特徵改變為投影系統所要之特徵。舉例而言,調節 光學器件422可改變光發散、光偏振態、光譜中之任何一 或夕種。5周卽光學器件422可包括(例如)一或多個透鏡、一 偏振轉換器、一預偏振器及/或一濾光器以移除不期望之 紫外線或紅外光。 光之X偏振組份由PBS 42〇反射至反射成像器426。反射 成像器426之液晶模式可為近晶型、向列型或某些其他合 適類型之反射成像器。若反射成像器426為近晶型,則反 射成像器426可為強誘電性液晶顯示器(Flcd)。反射成像 器426反射並調變具有y偏振之成像光束。經反射之y偏振 125223.doc -18- 200835936 光經PBS 420透射且由投影透鏡系統428投影,考慮到在投 影透鏡系統428與該(等)成像器之間的所有組件,投影透鏡 系統428之設計通常針對各特定光學系統而經最佳化。控 制器452與反射成像器426耦合以控制反射成像器426之運 作。通常,控制器452使反射成像器426之不同像素活化以 產生反射光之影像。 圖5示意性地說明多成像器投影系統5〇〇之一實施例。光 502係自光源504發出。光源504可為弧光燈或白熾燈或用 肇 於產生適用於投影景彡像之光之任何其他合適光源。光源 5 04可由諸如橢圓形反射器(如所展示)、拋物面反射器或其 類似物之反射器506環繞以增加引向投影引擎之光之量。 通常在將光502分成不同色帶之前對其進行處理。舉例 而言,可使光502穿過可選預偏振器5〇8,使得僅將具有所 要偏振之光引向投影引擎。預偏振器可呈反射偏振器之形 式,使得將不期望之偏振態之反射光重新引導至光源5〇4 φ 用以再循環。亦可使光502均化,使得投影引擎中之成像 器得以均勻地受照明。一種使光5〇2均化之方法為使光5〇2 穿過反射通道510,但應瞭解亦可使用其他方法來使光均 . 化。 - 在所說明實施例中,均化光512穿過第一透鏡514以減小 發散角。均化光512接著入射於可為(例如)介電薄膜濾光器 之第一色彩分離器516上。第一色彩分離器516將第一色帶 中之光518與其餘之光520分離。 可使第一色帶中之光518穿過第二透鏡522及視情況穿過 125223.doc -19- 200835936 第三透鏡523,以控制第一色帶中之光5 1 8入射於第一 pBS 524上之光束尺寸。光518自第一PBS 524傳至第一成像器 526。成像器526將經PBS 524透射之偏振態之影像光528反 射至X方塊色彩組合器530中。成像器526可包括一或多個 諸如延遲器元件之補償元件以提供額外偏振旋轉且藉此增 加影像光之對比度。 可使其餘之光520穿過第四透鏡532。其餘之光52〇接著 入射於第二色彩分離器534(例如薄膜濾光器或其類似物)上 以產生第二色帶中之光束53 6及第三色帶中之光束538。經 由第二PBS 542將第二色帶中之光束536引導至第二成像器 540。第二成像器540將第二色帶中之影像光544引導至X方 塊色彩組合器530中。 經由第三PBS 548將第三色帶中之光束538引導至第三成 像器546。第三成像器546將第三色帶中之影像光550引導 至X方塊色彩組合器530中。 第一、第二及第三色帶中之影像光528、544及550於X方 塊色彩組合器530中組合且作為全色影像光束被引導至投 影光學器件552。可在PBS 524、542及548與X方塊色彩組 合器530之間提供偏振旋轉光學器件554(例如半波延遲板 或其類似物)以控制於X方塊色彩組合器5 3 0中組合之光之 偏振。在所說明實施例中,將偏振旋轉光學器件554安置 於X方塊色彩組合器530與第一 PBS 524及第三PBS 548之 間。PBS 524、542及548中之任一者、兩者或所有三者可 包括一或多個如本文所述之多層反射偏振膜。 125223.doc -20- 200835936 w瞭解了使用所說明實施例之變體。舉例而言,pB$可 將光透射至成像器中且接著反射影像光,而不是將光反射 至成像裔中且接著透射影像光。上文所述之投影系統僅為 貝例’可設計多種利用本發明之多膜PBS之系統。 實例 所使用之聚酯多層反射偏振膜在結構上類似。黏著劑係 根據製造黏著劑之通用方法製造。當然,該等黏著劑中之 每一者均代表本發明之至少一種結晶抑制增塑劑組份之不 同實例。 實驗配置 總則 用將實質光聚焦至多層光學膜(MOF)(在PBS内)上之光 照射襄置測試PBS總成。PBS含有經設計以反射,,藍光"之 特定偏振之MOF膜。過濾入射光以傳遞在藍色範圍内之光 帶’其具有約434 nm之短波限及約514 nm之長波限(對於 指定波限而言透射率為5〇%)。入射於測試樣品上之光強度 之描述性量化係稱為強度比。該比率將測試PBS所經歷之 最雨瓦特/平方毫米數與參考背面投影電視中之PBS所經歷 之瓦特/平方毫米數相比。該瓦特/平方毫米’,經歷,,為由燈/ 光學器件組態傳遞至PBS之實際光強度與光傳播至pBS及 自PBS傳播之次數的組合。在吾等典型加速測試中,pBS 測試膜經歷約12倍於參考背面投影TV之PBS之光強度;此 係稱作”12x”測試,其中12x係指測試物與參考TV之間的此 強度比。強度比計算之進一步解釋可見於公開論文C.L. 125223.doc -21- 200835936Water; a diol and an aromatic or aliphatic moiety that interacts with water; and with the polymer that constitutes M〇F. In a preferred embodiment, the transparent adhesive tree used in the present application contains: or a plurality of epoxy resins up to about 99.5 weights based on the total weight of the composition. The epoxy resin composition of the present specification may comprise: or a plurality of from about 75% by weight to about % by weight based on the total weight of the composition. Oxygen resin. Further, the epoxy resin composition of the present invention may comprise about 94 weight percent of an epoxy resin based on the total weight of the composition. Lili. The plasticizer can be present in the permeable adhesive resin composition in an amount to prevent the formation of defects which are recorded in the desired period. VII. One of the crystallization inhibiting plasticizer components used in the adhesive material can be widely used, and the amount of fish is wide and lacks, but it is usually between about five and 30. Reset 〇/0 between the pots. 〆 & 于 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 'decane, antioxidants, free radicals 125223.doc 17- 200835936 Repellents, excited state inhibitors and uv absorbers and the like to reduce the weight and / or cost of the epoxy resin composition, adjust the viscosity, provide Additional reinforcement, improved transparency of the epoxy resin composition and optical assembly, and/or stabilization of the PB S assembly to avoid degradation. 4 illustrates an embodiment of an optical imager system in which system 4 includes a light source 412, such as an arc lamp 414 having a reflector 416 that directs light 418 forwardly. Light source 412 can also be a solid state light source such as a light emitting diode or a laser source. System 410 also includes a PBS 420, such as a single membrane or multi-membrane PBS as described herein. A light system having X polarization (i.e., polarized in a direction parallel to the X axis) is represented by a circled X. A light system having y polarization (i.e., polarization in a direction parallel to the y-axis) is indicated by a solid arrow. The solid line represents the incident light, and the dashed line represents the light that has been reflected back by the reflective imager 426 with a modified polarization state. The illumination optics 422 can be used to adjust the light provided by the source 412 prior to illuminating the PBS 420. The adjustment optics 422 changes the characteristics of the light emitted by the source 412 to the desired characteristics of the projection system. For example, conditioning optics 422 can change any of the divergence, optical polarization, and spectrum. The 5 week 卽 optics 422 can include, for example, one or more lenses, a polarization converter, a pre-polarizer, and/or a filter to remove unwanted ultraviolet or infrared light. The X-polarized component of light is reflected by PBS 42〇 to reflective imager 426. The liquid crystal mode of the reflective imager 426 can be a smectic, nematic or some other suitable type of reflective imager. If the reflective imager 426 is smectic, the reflective imager 426 can be a strongly induced liquid crystal display (Flcd). Reflective imager 426 reflects and modulates the imaging beam having y polarization. Reflected y-polarization 125223.doc -18- 200835936 Light is transmitted through PBS 420 and projected by projection lens system 428, taking into account all components between projection lens system 428 and the imager, projection lens system 428 The design is typically optimized for each particular optical system. Controller 452 is coupled to reflective imager 426 to control the operation of reflective imager 426. Typically, controller 452 activates the different pixels of reflective imager 426 to produce an image of the reflected light. FIG. 5 schematically illustrates one embodiment of a multi-imager projection system 5〇〇. Light 502 is emitted from light source 504. Light source 504 can be an arc or incandescent lamp or any other suitable source for generating light suitable for projecting a scene. Light source 504 may be surrounded by a reflector 506 such as an elliptical reflector (as shown), a parabolic reflector or the like to increase the amount of light directed to the projection engine. Light 502 is typically processed prior to being divided into different ribbons. For example, light 502 can be passed through optional pre-polarizer 5〇8 such that only light having the desired polarization is directed to the projection engine. The pre-polarizer can be in the form of a reflective polarizer such that the reflected light of the undesired polarization state is redirected to the source 5 〇 4 φ for recycling. Light 502 can also be homogenized such that the imager in the projection engine is evenly illuminated. One method of homogenizing the light 5〇2 is to pass the light 5〇2 through the reflective channel 510, but it should be understood that other methods can be used to homogenize the light. - In the illustrated embodiment, the homogenized light 512 passes through the first lens 514 to reduce the divergence angle. The homogenized light 512 is then incident on a first color separator 516, which may be, for example, a dielectric film filter. The first color separator 516 separates the light 518 in the first ribbon from the remaining light 520. The light 518 in the first ribbon can be passed through the second lens 522 and optionally through the 125223.doc -19-200835936 third lens 523 to control the light 5 1 8 in the first ribbon to be incident on the first pBS. Beam size on 524. Light 518 is transmitted from first PBS 524 to first imager 526. Imager 526 reflects the imaged light 528 of the polarization state transmitted through PBS 524 into X-square color combiner 530. Imager 526 can include one or more compensating elements, such as retarder elements, to provide additional polarization rotation and thereby increase the contrast of the image light. The remaining light 520 can be passed through the fourth lens 532. The remaining light 52 is then incident on a second color separator 534 (e.g., a thin film filter or the like) to produce a beam 53 in the second ribbon and a beam 538 in the third ribbon. Light beam 536 in the second ribbon is directed to second imager 540 via second PBS 542. The second imager 540 directs the image light 544 in the second ribbon to the X-block color combiner 530. Light beam 538 in the third ribbon is directed to third imager 546 via third PBS 548. The third imager 546 directs the image light 550 in the third ribbon to the X-square color combiner 530. Image light 528, 544, and 550 in the first, second, and third ribbons are combined in X-block color combiner 530 and directed to projection optics 552 as a full-color image beam. Polarization rotation optics 554 (eg, a half wave retarder or the like) may be provided between PBS 524, 542, and 548 and X block color combiner 530 to control the combined light in X-square color combiner 530 polarization. In the illustrated embodiment, polarization rotating optics 554 are disposed between X-square color combiner 530 and first PBS 524 and third PBS 548. Any, two or all of PBS 524, 542 and 548 may comprise one or more multilayer reflective polarizing films as described herein. 125223.doc -20- 200835936 w understands the use of variants of the illustrated embodiment. For example, pB$ can transmit light into the imager and then reflect the image light instead of reflecting the light into the imaged and then transmitting the image. The projection system described above is only a single example of a system that can utilize a multi-membrane PBS utilizing the present invention. EXAMPLE The polyester multilayer reflective polarizing film used is structurally similar. Adhesives are manufactured according to the general method of making adhesives. Of course, each of these adhesives represents a different example of at least one crystallization inhibiting plasticizer component of the present invention. Experimental Setup General The PBS assembly was tested with a light illuminating device that focused the substantial light onto a multilayer optical film (MOF) (in PBS). The PBS contains a MOF film designed to reflect, and blue light, a specific polarization. The incident light is filtered to deliver a band of light in the blue range' which has a short wavelength limit of about 434 nm and a long wavelength limit of about 514 nm (transmittance of 5〇% for a given wavelength limit). Descriptive quantification of the intensity of light incident on a test sample is referred to as the intensity ratio. This ratio compares the deadliest watts per square millimeter experienced by the test PBS to the watts per square millimeter experienced by the PBS in the reference rear projection television. The watts per square millimeter', experienced, is the combination of the actual light intensity delivered to the PBS by the lamp/optics configuration and the number of times light travels to and from the PBS. In our typical accelerated test, the pBS test film experienced about 12 times the light intensity of the PBS of the reference back projection TV; this is called the "12x" test, where 12x refers to this intensity ratio between the test object and the reference TV. . Further explanation of the intensity ratio calculation can be found in the public paper C.L. 125223.doc -21- 200835936
Bruzzone, J.J. Schneider,及 S.K. Eckhardt, "6.1 Photostability of Polymeric Cartesian Polarizing BeamBruzzone, J.J. Schneider, and S.K. Eckhardt, "6.1 Photostability of Polymeric Cartesian Polarizing Beam
Splitters1’,SID 04 Digest,第 60-63 頁(2004)中。 對於所有樣品而言,將PBS方塊總成之外部溫度人工地 控制至約42。(:。用肉眼觀察PBS,且亦經由在實驗期間週 期性地獲取之PB S總成之透射UV/可見光譜來監控該等 PBS。該等光譜允許b*(黃度之典型量化)之計算。藉由反 映在為3·75之b*色值中之不可接受的色彩改變來測定失 效。 除了精確調配差異以外,對於各樣品而言以類似方式混 合黏著劑。首先將添加劑溶解於以胺為主之固化劑中且接 著將混合物與環氧樹脂混合。將黏著劑靜置丨小時以移除 氣泡且接著用於建構PBS。對於所有樣品而言以同樣方式 建構PBS總成。該建構係由將定計量之黏著劑液滴塗覆至 出口稜鏡上、將膜敷設於黏著劑上、將黏著劑液滴塗覆至 膜上及用入口稜鏡覆蓋組成。藉由用丙酮輕微地擦栻表面 來清潔PBS且接著將總成在6〇°C烘箱中固化24小時。 樣品1至15 在1〇·2〇% RH之估計濕度下製備樣品1至15。該等實驗 樣品測試水及三種其他可能增塑劑之使用。將增塑劑混合 入以環氧樹脂為主之黏著劑(含有光穩定劑)中。增塑劑結 構展示如下: 實驗中使用增塑劑(非水)來延長加速壽命 125223.doc -22- 200835936Splitters 1', SID 04 Digest, pp. 60-63 (2004). The external temperature of the PBS square assembly was artificially controlled to about 42 for all samples. (: The PBS was visually observed, and the PBS was also monitored via the transmitted UV/visible spectrum of the PB S assembly periodically acquired during the experiment. The spectra allowed calculation of b* (typical quantification of yellowness) The failure was determined by an unacceptable color change reflected in the b* color value of 3.75. In addition to the precise blending difference, the adhesive was mixed in a similar manner for each sample. The additive was first dissolved in the amine. The main curing agent was then mixed with the epoxy resin. The adhesive was allowed to stand for an hour to remove the bubbles and then used to construct the PBS. The PBS assembly was constructed in the same manner for all samples. Applying a fixed amount of adhesive droplets to the exit crucible, applying the film to the adhesive, applying the adhesive droplets to the film, and covering with the inlet crucible. By wiping slightly with acetone The surface of the crucible was used to clean the PBS and the assembly was then cured in an oven at 6 ° C for 24 hours. Samples 1 to 15 Samples 1 to 15 were prepared at an estimated humidity of 1〇·2〇% RH. Three other possible plasticizers The plasticizer is mixed into an epoxy resin-based adhesive (containing a light stabilizer). The plasticizer structure is shown as follows: Plasticizer (non-water) is used in the experiment to prolong the accelerated life 125223.doc - 22- 200835936
下文列表中之數字數據分成四攔。”實際失效時間(小時 數)(AHTF)"為直至PBS總成顯影3 75之b*色彩為止所經過 之時間。”加速強度比("X"),,為測試樣品所經歷之平均光強 度相對於參考背面投影電視中之PBS所經歷之平均光強 度。"(AHTF)*("X")"為實際失效小時數乘以強度比。,,作 為對照樣品平均值之比率之估計壽命増加,,為樣品 (AHTF)*( X")與對照值平均值11461之比率。其為關於樣 品壽命多少倍於對照物壽命之量度。對照物係指未添加增 塑劑或未經處理之作為標準之膜及黏著劑,參見樣品工至 5。真空處理膜(參見樣品6及7)係指經受〇1托歷時2天且接 著立即用於建構PBS之膜。此真空處理意欲模擬在測試之 前經歷極乾燥條件之膜。 表1中之數據展示增塑劑延長PBS總成之加速壽命。含 有增塑劑之樣品提供對照物壽命之約12至16倍範圍内之 哥命。添加水至黏著劑中亦提供增加之壽命。在實際使用 中’ PBS將需要對背面投影7¥之壽命起到作用。認為具有 比水低之揮發性之增塑劑為重要工具,因為水濃度可經實 際使用時段隨環境改變。真空處理膜展示低於對照物之壽 命。此有助於展示缺水(增塑劑)對壽命有害。雖然環境: 度可使膜中之水濃度平衡,但是真空樣品展示此平衡並不' 125223.doc -23- 200835936 迅速以至於在加速測試持續期間内不能完全克服初始極 端乾燥之效應。 表1·多種樣品所提供之壽命 加速強度 比("X,,)The numerical data in the list below is divided into four blocks. The actual time to failure (hours) (AHTF)" is the time elapsed until the PBS assembly develops a b* color of 3 75." Acceleration intensity ratio ("X"), the average experienced by the test sample The light intensity is relative to the average light intensity experienced by the PBS in the reference rear projection television. "(AHTF)*("X")" is the actual failure hours multiplied by the intensity ratio. , as the estimated life of the ratio of the average of the control samples, is the ratio of the sample (AHTF)*(X") to the control value average of 11461. It is a measure of how many times the sample life is over the life of the control. The control refers to a film and an adhesive which are not added with a plasticizer or untreated, see sample work to 5. The vacuum treated membrane (see samples 6 and 7) refers to a membrane that was subjected to 〇 1 Torr for 2 days and immediately used to construct PBS. This vacuum treatment is intended to simulate a film that undergoes extremely dry conditions prior to testing. The data in Table 1 shows that the plasticizer extends the accelerated life of the PBS assembly. Samples containing plasticizers provide about 12 to 16 times the life of the control. The addition of water to the adhesive also provides an increased life. In actual use, PBS will need to play a role in the life of the rear projection 7¥. Plasticizers which are considered to have a lower volatility than water are important tools because the water concentration can vary with the environment over the actual period of use. The vacuum treated film exhibited a lower life than the control. This helps to show that water shortages (plasticizers) are detrimental to life. Although the environment: degree can balance the water concentration in the membrane, the vacuum sample shows that this balance is not '125223.doc -23- 200835936 so fast that the effect of the initial extreme drying cannot be completely overcome during the duration of the accelerated test. Table 1. Lifetime provided by various samples Accelerated intensity ratio ("X,,)
7 樣品1至6之 745 11.7 121 i含增 含有3重加 之水的樣3___τ 含添加至 含有ι〇ίϋ之添加至 之乙二哼的樣品 (AHTFV(,,ΧΠ) 14035 10258 9865 13634 11414 9663 11461 9015 745 1407 1620 1357 106 120 7897 16884 17496 16284 12 14 15 含有之添加至 二%樣品 τ 含有30重量%之添加至黏著劑中 ^£^(2-乙基己酯〇 3有20重臺^之添加至 樣品7 Samples 1 to 6 of 745 11.7 121 i containing a sample containing 3 additional water 3___τ containing a sample added to the containing yttrium containing ι〇ίϋ (AHTFV(,,ΧΠ) 14035 10258 9865 13634 11414 9663 11461 9015 745 1407 1620 1357 106 120 7897 16884 17496 16284 12 14 15 Adding to the second sample τ containing 30% by weight added to the adhesive ^ 2 ^ (2-ethylhexyl ester 〇 3 has 20 tables ^ Add to sample
含有20重量%之添加至黏著 之七雙的樣品 T20% by weight of sample added to the adhesive seven pairs T
106 13939 15912 1620 1811 104 10 16848 18110 參妝其中說明壽命對黃度之圖表(將pBs總成之壽命小時 數與b $度值相比)之圖6來說明使用根據本發明製得之多 層膜及黏著劑之pBS總成所提供之使用壽命顯著增加之一 κ例對於並未使用本發明之多層膜及黏著劑之pBS總成 125223.doc -24. 200835936 而言,黃化之開始發生於約750小時後。此與其中包括本 發明之結晶抑制增塑劑中之一者(亦即1 〇%乙二醇)之黏著 劑將黃化之開始延遲至約1300小時後的PBS總成的黃化形 成鮮明對比。 本發明可在沒有背離其精神及範疇之情況下採取多種修 改及變更。因此,本發明並不受限於其上述態樣,但將如 在以下申請專利範圍及其任何等效物中所闡明般受到控 制。 • 【圖式簡單說明】 圖1示意性地說明具有多層反射偏振膜之PB S之一實施 例; 圖2示意性地說明多層反射偏振膜及黏著劑之放大橫截 面; 圖3示意性地說明多層反射偏振膜之一部分的放大透視 _ , _ 圖4示意性地說明一投影系統; 圖5示意性地說明另一投影系統;及 圖6說明將具有一或多種黏著劑之pBS與不具有該(等)黏 • 著劑之PBS進行比較的圖表。 【主要元件符號說明】 10 偏振光束分光器總成 12 多層反射偏振膜 14 黏著層 16 稜鏡 125223.doc -25- 200835936106 13939 15912 1620 1811 104 10 16848 18110 Figure 6 illustrating the life versus yellowness chart (comparing the lifespan of the pBs assembly with the b $ value) Figure 6 illustrates the use of a multilayer film made in accordance with the present invention. And the service life of the pBS assembly of the adhesive is significantly increased by one κ. For the pBS assembly that does not use the multilayer film and adhesive of the present invention 125223.doc -24. 200835936, the beginning of the yellowing occurs in After about 750 hours. This is in sharp contrast to the yellowing of the PBS assembly after one of the crystallization inhibiting plasticizers of the present invention (i.e., 1% by weight of ethylene glycol) delays the onset of yellowing to about 1300 hours. . The invention can be modified and altered without departing from the spirit and scope of the invention. Therefore, the invention is not limited by the foregoing aspects, but is to be construed as being BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 schematically illustrates an embodiment of a PB S having a multilayer reflective polarizing film; FIG. 2 schematically illustrates an enlarged cross section of a multilayer reflective polarizing film and an adhesive; FIG. 3 schematically illustrates An enlarged perspective of a portion of a multilayer reflective polarizing film _, FIG. 4 schematically illustrates a projection system; FIG. 5 schematically illustrates another projection system; and FIG. 6 illustrates a pBS having one or more adhesives and without the (etc.) Sticky Pharmacy PBS for comparison chart. [Main component symbol description] 10 Polarized beam splitter assembly 12 Multi-layer reflective polarizing film 14 Adhesive layer 16 稜鏡 125223.doc -25- 200835936
18 黏著層 20 稜鏡 22 第一光透射層 22a 第一光透射層 22b 第一光透射層 22c 第一光透射層 24 第二光透射層 24a 第二光透射層 24b 第二光透射層 24c 第二光透射層 410 光學成像器系統 412 光源 414 弧光燈 416 反射器 418 光 420 PBS 422 調節光學器件 426 反射成像器 428 投影透鏡系統 452 控制器 500 多成像器投影系統 502 光 504 光源 506 反射器 125223.doc -26- 20083593618 adhesive layer 20 稜鏡 22 first light transmitting layer 22a first light transmitting layer 22b first light transmitting layer 22c first light transmitting layer 24 second light transmitting layer 24a second light transmitting layer 24b second light transmitting layer 24c Two Light Transmissive Layer 410 Optical Imager System 412 Light Source 414 Arc Light 416 Reflector 418 Light 420 PBS 422 Adjustment Optics 426 Reflection Imager 428 Projection Lens System 452 Controller 500 Multi Imager Projection System 502 Light 504 Light Source 506 Reflector 125223 .doc -26- 200835936
508 預偏振器 510 反射通道 512 均化光 514 第一透鏡 516 第一色彩分離器 518 光 520 其餘之光 522 第二透鏡 523 第三透鏡 524 第一 PBS 526 第一成像器 528 影像光 530 X方塊色彩組合器 532 第四透鏡 534 第二色彩分離器 536 光束 538 光束 540 第二成像器 542 第二 PBS 544 影像光 546 第三成像器 548 第三PBS 550 影像光 552 投影光學器件 125223.doc -27- 200835936 554 偏振旋轉光學器件 ^22x 折射率 n22y 折射率 n22z 折射率 ^24x 折射率 I^24y 折射率 ^24z 折射率 X 方向 Y 方向 z 方向508 pre-polarizer 510 reflective channel 512 homogenizing light 514 first lens 516 first color separator 518 light 520 remaining light 522 second lens 523 third lens 524 first PBS 526 first imager 528 image light 530 X square Color combiner 532 fourth lens 534 second color separator 536 beam 538 beam 540 second imager 542 second PBS 544 image light 546 third imager 548 third PBS 550 image light 552 projection optics 125223.doc -27 - 200835936 554 Polarization Rotating Optics ^22x Refractive Index n22y Refractive Index n22z Refractive Index ^24x Refractive Index I^24y Refractive Index ^24z Refractive Index X Direction Y Direction z Direction
125223.doc -28-125223.doc -28-
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-
2007
- 2007-09-25 EP EP07843124.4A patent/EP2074470B1/en not_active Not-in-force
- 2007-09-25 CN CN2007800359845A patent/CN101517457B/en not_active Expired - Fee Related
- 2007-09-25 WO PCT/US2007/079389 patent/WO2008042648A1/en not_active Ceased
- 2007-09-25 US US12/443,342 patent/US20100033816A1/en not_active Abandoned
- 2007-09-25 US US11/860,885 patent/US20080079903A1/en not_active Abandoned
- 2007-09-25 JP JP2009530555A patent/JP5676104B2/en not_active Expired - Fee Related
- 2007-09-25 KR KR1020097006375A patent/KR20090057289A/en not_active Withdrawn
- 2007-09-28 TW TW096136455A patent/TW200835936A/en unknown
-
2017
- 2017-05-08 US US15/589,657 patent/US10520744B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP2074470A1 (en) | 2009-07-01 |
| CN101517457B (en) | 2011-12-21 |
| US20080079903A1 (en) | 2008-04-03 |
| WO2008042648A1 (en) | 2008-04-10 |
| KR20090057289A (en) | 2009-06-04 |
| JP5676104B2 (en) | 2015-02-25 |
| EP2074470A4 (en) | 2016-02-24 |
| EP2074470B1 (en) | 2017-08-02 |
| US20100033816A1 (en) | 2010-02-11 |
| US10520744B2 (en) | 2019-12-31 |
| JP2010505148A (en) | 2010-02-18 |
| CN101517457A (en) | 2009-08-26 |
| US20170242265A1 (en) | 2017-08-24 |
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